Canonical Allele Identifier: CA2480925343

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571698T= , CM000663.2:g.154571698T=	GRCh38
NC_000001.10:g.154544174T= , CM000663.1:g.154544174T=	GRCh37
NC_000001.9:g.152810798T=	NCBI36
NG_008027.1:g.8918T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.875T= MANE Select	ENSP00000357461.3:p.Leu292=
ENST00000636034.1:c.875T=	ENSP00000489703.1:p.Leu292=
ENST00000637900.1:c.881T=	ENSP00000490474.1:p.Leu294=
ENST00000368476.3:c.875T=	ENSP00000357461.3:p.Leu292=
NM_000748.2:c.875T=	NP_000739.1:p.Leu292=
XM_017000180.2:c.365T=	XP_016855669.1:p.Leu122=
XR_001736952.2:n.1127T=
NM_000748.3:c.875T= MANE Select	NP_000739.1:p.Leu292=